Sorry my bad!!! I meant: --job=denovo,genome,draft,454 cheers Thomas On Jul 22, 2010, at 11:36 AM, Shabhonam Caim (TGAC) wrote: > Thanks thomas for your reply but still I am getting error: > I have used the following command and provided the qual file as well : > > mira --project=test --job=denovo,genome,draft 454_SETTINGS > -FN:fai=2.GAC.454Reads.fna -FN:fqui=2.GAC.454Reads.qual > > Minimum reads per group needed for tagging (mrpg) : [san] 2 > [454] 4 > Minimum neighbour quality needed for tagging (mnq) : [san] 20 > [454] 20 > Minimum Group Quality needed for RMB Tagging (mgqrt) : [san] 30 > [454] 25 > End-read Marking Exclusion Area in bases (emea) : [san] 25 > [454] 10 > Also mark gap bases (amgb) : [san] yes > [454] no > Also mark gap bases - even multicolumn (amgbemc) : [san] yes > [454] yes > Also mark gap bases - need both strands (amgbnbs): [san] yes > [454] yes > Force non-IUPAC consensus per sequencing type (fnicpst) : [san] no > [454] no > Merge short reads (msr) : [san] no > [454] no > Gap override ratio (gor) : [san] 66 > [454] 66 > > Edit options (-ED): > Automatic contig editing (ace) : [san] no > [454] yes > Sanger only: > Strict editing mode (sem) : no > Confirmation threshold in percent (ct) : 50 > > Directories (-DI): > When loading EXP files : > When loading SCF files : > Top directory for writing files : test_assembly > For writing result files : test_assembly/test_d_results > For writing result info files : test_assembly/test_d_info > For writing log files : test_assembly/test_d_log > For writing checkpoint files : test_assembly/test_d_chkpt > > File names (-FN): > When loading sequences from FASTA : [san] > test_in.sanger.fasta > [454] > 2.GAC.454Reads.fna > When loading qualities from FASTA quality : [san] > test_in.sanger.fasta.qual > [454] > 2.GAC.454Reads.qual > When loading sequences from FASTQ : [san] > test_in.sanger.fastq > [454] > test_in.454.fastq > When loading project from CAF : test_in.sanger.caf > When loading project from MAF (disabled) : test_in.sanger.maf > When loading EXP fofn : test_in.fofn > When loading project from PHD : test_in.phd.1 > When loading strain data : test_straindata_in.txt > When loading XML trace info files : [san] > test_traceinfo_in.sanger.xml > [454] > test_traceinfo_in.454.xml > When loading SSAHA vector screen results : > test_ssaha2vectorscreen_in.txt > > When loading backbone from MAF : test_backbone_in.maf > When loading backbone from CAF : test_backbone_in.caf > When loading backbone from GenBank : test_backbone_in.gbf > When loading backbone from FASTA : test_backbone_in.fasta > > > Output files (-OUTPUT/-OUT): > Save simple singlets in project (sssip) : [san] no > [454] no > Save tagged singlets in project (stsip) : [san] yes > [454] yes > > Remove rollover logs (rrol) : yes > Remove log directory (rld) : no > > Result files: > Saved as CAF (orc) : yes > Saved as FASTA (orf) : yes > Saved as GAP4 (directed assembly) (org) : no > Saved as phrap ACE (ora) : yes > Saved as HTML (orh) : no > Saved as Transposed Contig Summary (ors) : yes > Saved as simple text format (ort) : no > Saved as wiggle (orw) : yes > > Temporary result files: > Saved as CAF (otc) : yes > Saved as CAF (otm) : no > Saved as FASTA (otf) : no > Saved as GAP4 (directed assembly) (otg) : no > Saved as phrap ACE (ota) : no > Saved as HTML (oth) : no > Saved as Transposed Contig Summary (ots) : no > Saved as simple text format (ott) : no > > Extended temporary result files: > Saved as CAF (oetc) : no > Saved as FASTA (oetf) : no > Saved as GAP4 (directed assembly) (oetg) : no > Saved as phrap ACE (oeta) : no > Saved as HTML (oeth) : no > Save also singlets (oetas) : no > > Alignment output customisation: > TEXT characters per line (tcpl) : 60 > HTML characters per line (hcpl) : 60 > TEXT end gap fill character (tegfc) : > HTML end gap fill character (hegfc) : > > File / directory output names: > CAF : test_out.caf > MAF : test_out.maf > FASTA : test_out.unpadded.fasta > FASTA quality : test_out.unpadded.fasta.qual > FASTA (padded) : test_out.padded.fasta > FASTA qual.(pad): test_out.padded.fasta.qual > GAP4 (directory): test_out.gap4da > ACE : test_out.ace > HTML : test_out.html > Simple text : test_out.txt > TCS overview : test_out.tcs > Wiggle : test_out.wig > ------------------------------------------------------------------------------ > Deleting old directory test_assembly ... done. > Creating directory test_assembly ... done. > Creating directory test_assembly/test_d_log ... done. > Creating directory test_assembly/test_d_results ... done. > Creating directory test_assembly/test_d_info ... done. > Creating directory test_assembly/test_d_chkpt ... done. > Localtime: Thu Jul 22 10:31:49 2010 > > > > ========================== Memory self assessment > ============================== > Running in 64 bit mode. > > Dump from /proc/meminfo > -------------------------------------------------------------------------------- > MemTotal: 8174224 kB > MemFree: 94968 kB > Buffers: 4644 kB > Cached: 4976444 kB > SwapCached: 287504 kB > Active: 6618732 kB > Inactive: 1307228 kB > HighTotal: 0 kB > HighFree: 0 kB > LowTotal: 8174224 kB > LowFree: 94968 kB > SwapTotal: 2031608 kB > SwapFree: 1476740 kB > Dirty: 1984 kB > Writeback: 0 kB > AnonPages: 2936468 kB > Mapped: 32408 kB > Slab: 81840 kB > PageTables: 37252 kB > NFS_Unstable: 0 kB > Bounce: 0 kB > CommitLimit: 6118720 kB > Committed_AS: 5290616 kB > VmallocTotal: 34359738367 kB > VmallocUsed: 263728 kB > VmallocChunk: 34359474579 kB > HugePages_Total: 0 > HugePages_Free: 0 > HugePages_Rsvd: 0 > Hugepagesize: 2048 kB > -------------------------------------------------------------------------------- > > Dump from /proc/self/status > -------------------------------------------------------------------------------- > Name: mira > State: R (running) > SleepAVG: 0% > Tgid: 6158 > Pid: 6158 > PPid: 17617 > TracerPid: 0 > Uid: 8395 8395 8395 8395 > Gid: 3658 3658 3658 3658 > FDSize: 256 > Groups: 3658 > VmPeak: 4972 kB > VmSize: 4920 kB > VmLck: 0 kB > VmHWM: 1744 kB > VmRSS: 1744 kB > VmData: 464 kB > VmStk: 84 kB > VmExe: 4336 kB > VmLib: 0 kB > VmPTE: 28 kB > StaBrk: 00a7e000 kB > Brk: 017f0000 kB > StaStk: 7fffc798fa70 kB > Threads: 1 > SigQ: 0/71680 > SigPnd: 0000000000000000 > ShdPnd: 0000000000000000 > SigBlk: 0000000000000000 > SigIgn: 0000000000000000 > SigCgt: 0000000180000000 > CapInh: 0000000000000000 > CapPrm: 0000000000000000 > CapEff: 0000000000000000 > Cpus_allowed: > 00000000,00000000,00000000,00000000,00000000,00000000,00000000,000000ff > Mems_allowed: 00000000,00000001 > -------------------------------------------------------------------------------- > > Information on current assembly object: > > AS_readpool: 0 reads. > AS_contigs: 0 contigs. > AS_bbcontigs: 0 contigs. > Mem used for reads: 112 (112 B) > > Memory used in assembly structures: > Eff. Size Free cap. LostByAlign > AS_writtenskimhitsperid: 0 24 B 0 B 0 B > AS_skim_edges: 0 24 B 0 B 0 B > AS_adsfacts: 0 24 B 0 B 0 B > AS_confirmed_edges: 0 24 B 0 B 0 B > AS_permanent_overlap_bans: 0 24 B 0 B 0 B > AS_readhitmiss: 0 24 B 0 B 0 B > AS_readhmcovered: 0 24 B 0 B 0 B > AS_count_rhm: 0 24 B 0 B 0 B > AS_clipleft: 0 24 B 0 B 0 B > AS_clipright: 0 24 B 0 B 0 B > AS_used_ids: 0 24 B 0 B 0 B > AS_multicopies: 0 24 B 0 B 0 B > AS_hasmcoverlaps: 0 24 B 0 B 0 B > AS_maxcoveragereached: 0 24 B 0 B 0 B > AS_coverageperseqtype: 0 24 B 0 B 0 B > AS_istroublemaker: 0 24 B 0 B 0 B > AS_isdebris: 0 24 B 0 B 0 B > AS_needalloverlaps: 0 40 B 0 B 0 B > AS_readsforrepeatresolve: 0 40 B 0 B 0 B > AS_allrmbsok: 0 24 B 0 B 0 B > AS_probablermbsnotok: 0 24 B 0 B 0 B > AS_weakrmbsnotok: 0 24 B 0 B 0 B > AS_readmaytakeskim: 0 40 B 0 B 0 B > AS_skimstaken: 0 40 B 0 B 0 B > AS_numskimoverlaps: 0 24 B 0 B 0 B > AS_numleftextendskims: 0 24 B 0 B 0 B > AS_rightextendskims: 0 24 B 0 B 0 B > AS_skimleftextendratio: 0 24 B 0 B 0 B > AS_skimrightextendratio: 0 24 B 0 B 0 B > AS_usedlogfiles: 1 48 B 0 B 0 B > Total: 920 (920 B) > > ================================================================================ > Dynamic allocs: 0 > Align allocs: 0 > > Fatal Error (may be due to problems of the input data): > "You did not specify any input sequences to be loaded." > > ->Thrown: void Assembly::loadSequenceData_new() > > ->Caught: main > > Cheers > Shab > > > From: mira_talk-bounce@xxxxxxxxxxxxx [mailto:mira_talk-bounce@xxxxxxxxxxxxx] > On Behalf Of Thomas Müller > Sent: 22 July 2010 10:12 > To: mira_talk@xxxxxxxxxxxxx > Subject: [mira_talk] Re: FW: 454 assembly > > try: > mira --project=test --job=denovo,genome,draft,est 454_SETTINGS > -FN:fai=2.GAC.454Reads.fna > > But you should really also add the .qual file with FN:fqui=2.GAC.454Reads.qual > > cheers > Thomas > > On Jul 22, 2010, at 10:53 AM, Shabhonam Caim (TGAC) wrote: > > > > Hello Mira Users > > I am trying to assemble the 454 reads using Mira by using following command: > mira-3.0.0 mira --project=test --job=denovo,genome,draft,2.GAC.454Reads.fna > > and I am getting the following error: > > This is MIRA V3.0.0 (production version). > > Please cite: Chevreux, B., Wetter, T. and Suhai, S. (1999), Genome Sequence > Assembly Using Trace Signals and Additional Sequence Information. > Computer Science and Biology: Proceedings of the German Conference on > Bioinformatics (GCB) 99, pp. 45-56. > > Mail general questions to the MIRA talk mailing list: > mira_talk@xxxxxxxxxxxxx > > To (un-)subsubcribe the MIRA mailing lists, see: > http://www.chevreux.org/mira_mailinglists.html > > To report bugs or ask for features, please use the new ticketing system at: > http://sourceforge.net/apps/trac/mira-assembler/ > This ensures that requests don't get lost. > > > Compiled by: bach > Sun Jan 31 20:23:36 CET 2010 > On: Linux arcadia64 2.6.27-11-generic #1 SMP Wed Apr 1 20:53:41 UTC 2009 > x86_64 GNU/Linux > Compiled in boundtracking mode. > Compiled in bugtracking mode. > Compilation settings (sorry, for debug): > Size of size_t : 8 > Size of uint32 : 4 > Size of uint32_t: 4 > Size of uint64 : 8 > Size of uint64_t: 8 > Current system: Linux n57140 2.6.18-92.el5 #1 SMP Tue Apr 29 13:16:15 EDT > 2008 x86_64 x86_64 x86_64 GNU/Linux > > > > Parsing parameters: --project=454asembly --job=denovo, genome, draft > pk.454.fasta > > Seen no assembly quality in job definition, assuming 'normal'. > Seen no assembly type in job definition, assuming 'genome'. > > ,.. > > ========================= Parameter parsing error(s) > ========================== > > * Parameter section: '(none)' > * unrecognised string or unexpected character: genome > > * Parameter section: '(none)' > * unrecognised string or unexpected character: draft > > * Parameter section: '(none)' > * unrecognised string or unexpected character: pk > > * Parameter section: '(none)' > * unrecognised string or unexpected character: 454 > > * Parameter section: '(none)' > * unrecognised string or unexpected character: fasta > > =============================================================================== > > Fatal Error (may be due to problems of the input data): > "Error while parsing parameters, sorry." > > ->Thrown: void MIRAParameters::parse(istream & is, vector<MIRAParameters> & > Pv, MIRAParameters * singlemp) > > ->Caught: main > > Or can I please get the commands to run the 454 assembly (basic denovo > assembly with default parameters) > > cheers > > Shab > > > -- > Crop Plant Biodiversity and Breeding Informatics Group (350b) > Institute of Plant Breeding, Seed Science and Population Genetics > University of Hohenheim > Fruwirthstrasse 21 > D-70599 Stuttgart > Phone: +49-711-459 24293 > -- Crop Plant Biodiversity and Breeding Informatics Group (350b) Institute of Plant Breeding, Seed Science and Population Genetics University of Hohenheim Fruwirthstrasse 21 D-70599 Stuttgart Phone: +49-711-459 24293